DMAPA chloride | Solubility of Things

Identification

Molecular formula

C₁₃H₂₆ClNO

CAS number

6786-83-2

IUPAC name

dimethyl-[3-(3,5,7-trimethyl-2-oxo-3H-azepin-1-yl)propyl]ammonium;chloride

State

At room temperature, DMAPA chloride is a liquid. Its hygroscopic nature means it can readily absorb water vapor from the atmosphere, and it is commonly handled as a solution.

Melting point (Celsius)

-40.00

Melting point (Kelvin)

233.15

Boiling point (Celsius)

184.00

Boiling point (Kelvin)

457.15

General information

Molecular weight

262.82g/mol

Molar mass

262.8190g/mol

Density

1.0203g/cm³

Appearence

DMAPA chloride is typically a colorless to pale yellow liquid. It is hygroscopic, meaning it can absorb moisture from the air, and is often available in an aqueous or slightly viscous solution form.

Comment on solubility

Solubility of Dimethyl-[3-(3,5,7-trimethyl-2-oxo-3H-azepin-1-yl)propyl]ammonium;chloride

The solubility of dimethyl-[3-(3,5,7-trimethyl-2-oxo-3H-azepin-1-yl)propyl]ammonium;chloride is an intriguing aspect of its chemical characterization, particularly due to its unique molecular structure. Here are some important points concerning its solubility:

Water Solubility: This compound is likely to have good solubility in water due to the presence of the ammonium group, which can interact favorably with water molecules.
Solubility in Organic Solvents: It may exhibit variable solubility in organic solvents. The presence of bulky hydrophobic groups might hinder solubility in non-polar solvents, while polar solvents could enhance solubility.
Hydration and Delocalization: Potential for hydration around the ammonium ion increases solubility, as water molecules can stabilize charged species.

In consideration of the above factors, it can be said that the solubility of this compound is influenced by both polar and non-polar interactions, making its behavior in various solvents quite complex. As Solubility is often a decisive factor in the development of pharmaceuticals and other applications, understanding the solubility profile of this compound is of paramount importance.

Interesting facts

Exploring Dimethyl-[3-(3,5,7-trimethyl-2-oxo-3H-azepin-1-yl)propyl]ammonium Chloride

Dimethyl-[3-(3,5,7-trimethyl-2-oxo-3H-azepin-1-yl)propyl]ammonium chloride is a fascinating compound that combines elements of organic chemistry and medicinal research. Here are some engaging facts about this intriguing compound:

Dual Functionality: This compound features both a quaternary ammonium group and a unique azepin structure, making it a candidate for applications in pharmaceuticals and biological research.
Structure and Stability: The incorporation of the azepin ring contributes to the compound's stability, which is significant for drug design and delivery systems.
Biological Activity: Compounds like this have been explored for their potential roles as antimicrobial agents, highlighting the importance of structural modifications in enhancing bioactivity.
Synthetic Applications: The synthesis of azepines has gained interest due to their usefulness in constructing more complex structures for medicinal chemistry.
Research Directions: Studies on this compound can pave the way for discovering new therapeutic agents, especially due to its ability to interact with various biological targets.

Incorporating such remarkable structural features, dimethyl-[3-(3,5,7-trimethyl-2-oxo-3H-azepin-1-yl)propyl]ammonium chloride offers promising avenues for researchers in the fields of chemistry and pharmacology.

As noted by research leaders in the field, “The synthesis and exploration of complex organic compounds like this represent the forefront of innovative therapeutic development.” This underscores the excitement that surrounds the study of such compounds, as they may hold the key to the next generation of remedial solutions.

Synonyms

2H-Azepin-2-one, 1,3-dihydro-1-(3-dimethylaminopropyl)-3,5,7-trimethyl-, hydrochloride

1-(3-Dimethylaminopropyl)-1,3-dihydro-3,5,7-trimethyl-2H-azepin-2-one hydrochloride

1676-28-4